Atenolol
- Product NDC
- 55700-661
- 11-digit product format
- 557000661
- Labeler code
- 55700
- Product ID
- 55700-661_dc52592d-0d7d-4815-8f3d-30b5ac4ed1c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2018-07-26
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-661-30 | 55700066130 | 30 TABLET in 1 BOTTLE (55700-661-30) | 30 tablet | 2019-03-15 | 0000-00-00 | No | No | Current |
| 55700-661-90 | 55700066190 | 90 TABLET in 1 BOTTLE (55700-661-90) | 90 tablet | 2018-07-26 | 0000-00-00 | No | No | Current |